Association of BCL11A genetic variant (rs11886868) with severity in β-thalassaemia major & sickle cell anaemia

Association of BCL11A genetic variant (rs11886868) with severity in β-thalassaemia major & sickle cell anaemia

Background & objectives: The amount of foetal haemoglobin that persists in adulthood affects the clinical severity of haemoglobinopathies including β-thalassaemia major and sickle cell anaemia (SCA). The present study was undertaken to analyse β-thalassaemia as well as SCA patients for the singl...

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Bibliographic Details
Main Authors: Sneha Dadheech, D Madhulatha, Suman Jainc, James Joseph, A Jyothy, Anjana Munshi
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Indian Journal of Medical Research
Subjects:
β-thalassaemia - erythroid precursors - foetal haemoglobin - sickle cell anaemia - single nucleotide polymorphisms (SNPs)
Online Access:http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2016;volume=143;issue=4;spage=449;epage=454;aulast=Dadheech

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http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2016;volume=143;issue=4;spage=449;epage=454;aulast=Dadheech

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